Disease #05796 (CSS10 (Coffin-Siris syndrome, type 10 (CSS10)), OMIM:618506)
| Official abbreviation |
CSS10 |
| Name |
Coffin-Siris syndrome, type 10 (CSS10) |
| OMIM ID |
618506 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
SOX4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-07-25 09:05:48 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|